Full-Time

Associate Principal Scientist

Statistical Programmer, Oncology

Confirmed live in the last 24 hours

MSD

MSD

Compensation Overview

$135.5k - $213.4kAnnually

Senior, Expert

H1B Sponsorship Available

North Wales, PA, USA + 1 more

More locations: Linden, NJ, USA

Hybrid work requiring three days on-site per week.

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Required Skills
Data Analysis

You match the following MSD's candidate preferences

Employers are more likely to interview you if you match these preferences:

Degree
Experience
Requirements
  • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment.
  • MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 7 or more years SAS programming experience in a clinical trial environment.
  • Excellent interpersonal skills and ability to negotiate and collaborate effectively.
  • Excellent written, oral, and presentation skills
  • Broad knowledge and significant experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)
  • Strong project management skills; leadership at a program level; determines approach and ensures consistency and directs development of others when opportunities arise; ability to engage key stakeholders.
  • Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise.
  • Experience leading large and/or complex statistical programming projects that include coordinating the activities of a programming team.
  • US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development of electronic submission deliverables.
  • Designs and develops complex programming algorithms.
  • Ability to comprehend analysis plans which may describe methodology to be programmed, an understanding of statistical terminology and concepts.
  • Familiarity with clinical data management concepts
  • Experience in CDISC and ADaM standards
  • Demonstrated success in the assurance of deliverable quality and process compliance.
  • Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices.
  • Ability to anticipate stakeholder requirements.
Responsibilities
  • Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices.
  • Maintain and manage a project plan including resource forecasting.
  • Coordinate the activities of a global programming team that includes outsource provider staff.
  • Membership on departmental strategic initiative teams.

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A